A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845251



Internal ID22620186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34439857..34470036hg38UCSC Ensembl
chr6:34407634..34437813hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3830180
hg1930180
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505321
Samples
Known GenesPACSIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845251
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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